A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222977



Internal ID22366879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79699322..79699427hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3671n152
Supporting Variantsnssv14282533, nssv14282531, nssv14282530, nssv14282534, nssv14282535, nssv14282532
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222977
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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